A high‐throughput screening assay to identify bacterial antagonists against Fusarium verticillioides. (21st June 2013)

• Record Type: Journal Article
• Authors: Figueroa‐López, Alejandro Miguel; Cordero‐Ramírez, Jesús Damián; Quiroz‐Figueroa, Francisco Roberto; Maldonado‐Mendoza, Ignacio Eduardo
• Is Part Of: Journal of basic microbiology. Volume 54:issue 1(2014:Jan.)
• Page Start: S125
• Page End: S133
• Publication Date: 2013-06-21
• Subjects: Microbiology -- Periodicals; 579
• DOI: 10.1002/jobm.201200594
• Languages: English
• ISSNs: 0233-111X

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="jobm201200594-sec-0001" sec-type="section"> <p>A high‐throughput antagonistic assay was developed to screen for bacterial isolates capable of controlling the maize fungal phytopathogen <italic>Fusarium verticillioides</italic>. This assay combines a straightforward methodology, in which the fungus is challenged with bacterial isolates in liquid medium, with a novel approach that uses the plant lectin wheat germ agglutinin (WGA) coupled to a fluorophore (Alexa‐Fluor® 488) under the commercial name of WGA, Alexa Fluor® 488 conjugate. The assay is performed in a 96‐well plate format, which reduces the required laboratory space and streamlines quantitation and automation of the process, making it fast and accurate. The basis of our assay is that fungal biomass can be assessed by WGA, Alexa Fluor® 488 conjugate staining, which recognizes the chitin in the fungal cell wall and thus permits the identification of potential antagonistic bacteria that inhibit fungal growth. This principle was validated by chitin‐competition binding assays against WGA, Alexa Fluor® 488 conjugate; confocal laser microscopy confirmed that the fluorescent WGA, Alexa Fluor® 488 conjugate binds to the chitin of the fungal cell wall. The majority of bacterial isolates did not bind to the WGA, Alexa Fluor® 488 conjugate. Furthermore, including washing steps significantly reduced any bacterial staining to background levels, even in the rare cases where bacterial isolates were capable of binding to WGA. Confirmatory conventional agar plate antagonistic assays were also conducted to validate our technique. We are now successfully employing this large‐scale antagonistic assay as a pre‐screening step for potential fungal antagonists in extensive bacteria collections (on the order of thousands of isolates).</p> </sec> </abstract>